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ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant

Disease Summary
Associated Targets (3)
Tbio

3


GARD Rare
Uniprot Description A form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. It is an autosomal dominant condition characterized by hypotrichosis, abnormal or missing teeth, and hypohidrosis due to the absence of sweat glands.
Mondo Term and Equivalent IDs
MONDO:0007509:  ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant
DOID:0111663: 
GARD:0002048: 
UMLS:C3888065: